IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
01 1IOL Chemicals and Pharmaceuticals Ltd.
02 3Granules India Limited
03 1Adare Pharmaceuticals, Inc.
04 1Asclemed USA Inc.
05 5BASF Corporation
06 1BASF SE
07 1Fagron Inc
08 1Fagron Services B.V.
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13 1Particle Dynamics International, LLC
14 2Professional Compounding Centers of America
15 1Professional Compounding Centers of America dba PCCA
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01 1COMPRESSO IBU 85 PAR
02 2Dexibuprofen
03 6IBUPROFEN
04 1IBUPROFEN DC85W
05 20Ibuprofen
06 2Ibuprofen Directly compressible granules 66%
07 1Racemic Ibuprofen Lysinate
01 6China
02 6Germany
03 7India
04 2Ireland
05 2Netherlands
06 7U.S.A
07 3United Kingdom
NDC Package Code : 49716-325
Start Marketing Date : 2017-06-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-300
Start Marketing Date : 2011-02-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (66mg/100mg)
Marketing Category : DRUG FOR FURTHER PROCESSING
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-303
Start Marketing Date : 2019-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (85mg/100mg)
Marketing Category : DRUG FOR FURTHER PROCESSING
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-311
Start Marketing Date : 2015-09-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (66mg/100mg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 10117-0926
Start Marketing Date : 2010-06-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10117-0930
Start Marketing Date : 2010-06-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 10117-0931
Start Marketing Date : 2014-01-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10117-0936
Start Marketing Date : 2010-06-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0406-3823
Start Marketing Date : 2013-02-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (0.63kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 0406-3825
Start Marketing Date : 2013-02-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (0.9kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
A (?)-Ibuprofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (?)-Ibuprofen, including repackagers and relabelers. The FDA regulates (?)-Ibuprofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (?)-Ibuprofen API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of (?)-Ibuprofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (?)-Ibuprofen supplier is an individual or a company that provides (?)-Ibuprofen active pharmaceutical ingredient (API) or (?)-Ibuprofen finished formulations upon request. The (?)-Ibuprofen suppliers may include (?)-Ibuprofen API manufacturers, exporters, distributors and traders.
click here to find a list of (?)-Ibuprofen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing (?)-Ibuprofen as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for (?)-Ibuprofen API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture (?)-Ibuprofen as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain (?)-Ibuprofen and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a (?)-Ibuprofen NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of (?)-Ibuprofen suppliers with NDC on PharmaCompass.
We have 18 companies offering (?)-Ibuprofen
Get in contact with the supplier of your choice:
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